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Last Name
Institution

David Randolph Beier, Ph.D., M.D.

TitleVisiting Professor of Medicine
InstitutionBrigham and Women's Hospital
DepartmentMedicine
AddressBrigham and Women's Hospital
Genetics Division, NRB, Room 458 C
77 Avenue Louis Pasteur
Boston MA 02115
Phone617/525-4715
Fax617/525-4705

 Bibliographic 
 selected publications
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Favero CB, Henshaw RN, Grimsley-Myers CM, Shrestha A, Beier DR, Dwyer ND. Mutation of the BiP/GRP78 gene causes axon outgrowth and fasciculation defects in the thalamocortical connections of the mammalian forebrain. J Comp Neurol. 2013 Feb 15; 521(3):677-96.
    View in: PubMed
  2. Manning DK, Sergeev M, van Heesbeen RG, Wong MD, Oh JH, Liu Y, Henkelman RM, Drummond I, Shah JV, Beier DR. Loss of the ciliary kinase nek8 causes left-right asymmetry defects. J Am Soc Nephrol. 2013 Jan; 24(1):100-12.
    View in: PubMed
  3. Tao J, Koster MI, Harrison W, Moran JL, Beier DR, Roop DR, Overbeek PA. A spontaneous fatp4/scl27a4 splice site mutation in a new murine model for congenital ichthyosis. PLoS One. 2012; 7(11):e50634.
    View in: PubMed
  4. Velupillai P, Sung CK, Andrews E, Moran J, Beier D, Kagan J, Benjamin T. Polymorphisms in toll-like receptor 4 underlie susceptibility to tumor induction by the mouse polyomavirus. J Virol. 2012 Nov; 86(21):11541-7.
    View in: PubMed
  5. Liem KF, Ashe A, He M, Satir P, Moran J, Beier D, Wicking C, Anderson KV. The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking. J Cell Biol. 2012 Jun 11; 197(6):789-800.
    View in: PubMed
  6. Retraction. Autoimmunity as the consequence of a spontaneous mutation in Rasgrp1. Immunity. 2012 May 25; 36(5):886.
    View in: PubMed
  7. Leshchiner I, Alexa K, Kelsey P, Adzhubei I, Austin-Tse CA, Cooney JD, Anderson H, King MJ, Stottmann RW, Garnaas MK, Ha S, Drummond IA, Paw BH, North TE, Beier DR, Goessling W, Sunyaev SR. Mutation mapping and identification by whole-genome sequencing. Genome Res. 2012 Aug; 22(8):1541-8.
    View in: PubMed
  8. Andrews E, Velupillai P, Sung CK, Beier DR, Benjamin T. Production of a natural antibody to the mouse polyoma virus is a multigenic trait. G3 (Bethesda). 2012 Mar; 2(3):353-5.
    View in: PubMed
  9. Weiss J, Hurley LA, Harris RM, Finlayson C, Tong M, Fisher LA, Moran JL, Beier DR, Mason C, Jameson JL. ENU mutagenesis in mice identifies candidate genes for hypogonadism. Mamm Genome. 2012 Jun; 23(5-6):346-55.
    View in: PubMed
  10. Stottmann RW, Turbe-Doan A, Tran P, Kratz LE, Moran JL, Kelley RI, Beier DR. Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivo. PLoS Genet. 2011 Sep; 7(9):e1002224.
    View in: PubMed
  11. Cozzi E, Ackerman KG, Lundequist A, Drazen JM, Boyce JA, Beier DR. The naive airway hyperresponsiveness of the A/J mouse is Kit-mediated. Proc Natl Acad Sci U S A. 2011 Aug 2; 108(31):12787-92.
    View in: PubMed
  12. Zheng Y, Yin H, Boeglin WE, Elias PM, Crumrine D, Beier DR, Brash AR. Lipoxygenases mediate the effect of essential fatty acid in skin barrier formation: a proposed role in releasing omega-hydroxyceramide for construction of the corneocyte lipid envelope. J Biol Chem. 2011 Jul 8; 286(27):24046-56.
    View in: PubMed
  13. Stottmann RW, Moran JL, Turbe-Doan A, Driver E, Kelley M, Beier DR. Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse. Genetics. 2011 Jul; 188(3):615-24.
    View in: PubMed
  14. Dwyer ND, Manning DK, Moran JL, Mudbhary R, Fleming MS, Favero CB, Vock VM, O'Leary DD, Walsh CA, Beier DR. A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype. Neural Dev. 2011; 6:3.
    View in: PubMed
  15. Bjork BC, Fujiwara Y, Davis SW, Qiu H, Saunders TL, Sandy P, Orkin S, Camper SA, Beier DR. A transient transgenic RNAi strategy for rapid characterization of gene function during embryonic development. PLoS One. 2010; 5(12):e14375.
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  16. Beier DR. New genetic resources for mammalian developmental biologists. F1000 Biol Rep. 2010; 2:72.
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  17. Hellman NE, Liu Y, Merkel E, Austin C, Le Corre S, Beier DR, Sun Z, Sharma N, Yoder BK, Drummond IA. The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretch. Proc Natl Acad Sci U S A. 2010 Oct 26; 107(43):18499-504.
    View in: PubMed
  18. Kamp A, Peterson MA, Svenson KL, Bjork BC, Hentges KE, Rajapaksha TW, Moran J, Justice MJ, Seidman JG, Seidman CE, Moskowitz IP, Beier DR. Genome-wide identification of mouse congenital heart disease loci. Hum Mol Genet. 2010 Aug 15; 19(16):3105-13.
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  19. Stottmann RW, Bjork BC, Doyle JB, Beier DR. Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse. Genesis. 2010 May; 48(5):303-8.
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  20. Shiba D, Manning DK, Koga H, Beier DR, Yokoyama T. Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia. Cytoskeleton (Hoboken). 2010 Feb; 67(2):112-9.
    View in: PubMed
  21. Smits P, Bolton AD, Funari V, Hong M, Boyden ED, Lu L, Manning DK, Dwyer ND, Moran JL, Prysak M, Merriman B, Nelson SF, Bonafé L, Superti-Furga A, Ikegawa S, Krakow D, Cohn DH, Kirchhausen T, Warman ML, Beier DR. Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210. N Engl J Med. 2010 Jan 21; 362(3):206-16.
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  22. Stottmann RW, Beier DR. Using ENU mutagenesis for phenotype-driven analysis of the mouse. Methods Enzymol. 2010; 477:329-48.
    View in: PubMed
  23. Bjork BC, Turbe-Doan A, Prysak M, Herron BJ, Beier DR. Prdm16 is required for normal palatogenesis in mice. Hum Mol Genet. 2010 Mar 1; 19(5):774-89.
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  24. Heydemann A, Ceco E, Lim JE, Hadhazy M, Ryder P, Moran JL, Beier DR, Palmer AA, McNally EM. Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice. J Clin Invest. 2009 Dec; 119(12):3703-12.
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  25. Douglas DS, Moran JL, Bermingham JR, Chen XJ, Brindley DN, Soliven B, Beier DR, Popko B. Concurrent Lpin1 and Nrcam mouse mutations result in severe peripheral neuropathy with transitory hindlimb paralysis. J Neurosci. 2009 Sep 30; 29(39):12089-100.
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  26. Stottmann RW, Tran PV, Turbe-Doan A, Beier DR. Ttc21b is required to restrict sonic hedgehog activity in the developing mouse forebrain. Dev Biol. 2009 Nov 1; 335(1):166-78.
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  27. Pettitt SJ, Liang Q, Rairdan XY, Moran JL, Prosser HM, Beier DR, Lloyd KC, Bradley A, Skarnes WC. Agouti C57BL/6N embryonic stem cells for mouse genetic resources. Nat Methods. 2009 Jul; 6(7):493-5.
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  28. Fernandez L, Marchuk DA, Moran JL, Beier DR, Rockman HA. An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15. Mamm Genome. 2009 May; 20(5):296-304.
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  29. Beckstead WA, Bjork BC, Stottmann RW, Sunyaev S, Beier DR. SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs. Mamm Genome. 2008 Oct-Dec; 19(10-12):687-90.
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  30. Seale P, Bjork B, Yang W, Kajimura S, Chin S, Kuang S, Scimè A, Devarakonda S, Conroe HM, Erdjument-Bromage H, Tempst P, Rudnicki MA, Beier DR, Spiegelman BM. PRDM16 controls a brown fat/skeletal muscle switch. Nature. 2008 Aug 21; 454(7207):961-7.
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  31. Tran PV, Haycraft CJ, Besschetnova TY, Turbe-Doan A, Stottmann RW, Herron BJ, Chesebro AL, Qiu H, Scherz PJ, Shah JV, Yoder BK, Beier DR. THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia. Nat Genet. 2008 Apr; 40(4):403-10.
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  32. Sohara E, Luo Y, Zhang J, Manning DK, Beier DR, Zhou J. Nek8 regulates the expression and localization of polycystin-1 and polycystin-2. J Am Soc Nephrol. 2008 Mar; 19(3):469-76.
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  33. Trapp ML, Galtseva A, Manning DK, Beier DR, Rosenblum ND, Quarmby LM. Defects in ciliary localization of Nek8 is associated with cystogenesis. Pediatr Nephrol. 2008 Mar; 23(3):377-87.
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  34. Kubo E, Fatma N, Akagi Y, Beier DR, Singh SP, Singh DP. TAT-mediated PRDX6 protein transduction protects against eye lens epithelial cell death and delays lens opacity. Am J Physiol Cell Physiol. 2008 Mar; 294(3):C842-55.
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  35. Leder A, McMenamin J, Zhou F, Moran JL, Beier DR, Leder P. Genome-wide SNP analysis of Tg.AC transgenic mice reveals an oncogenic collaboration between v-Ha-ras and Ink4a, which is absent in p53 deficiency. Oncogene. 2008 Apr 10; 27(17):2456-65.
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  36. Poirier C, Moran JL, Kovanci E, Petit DC, Beier DR, Bishop CE. Three loci on mouse chromosome 5 and 10 modulate sex determination in XX Ods/+ mice. Genesis. 2007 Jul; 45(7):452-5.
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  37. Matera I, Cockroft JL, Moran JL, Beier DR, Goldowitz D, Pavan WJ. A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3. Pigment Cell Res. 2007 Jun; 20(3):210-5.
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  38. Moran JL, Qiu H, Turbe-Doan A, Yun Y, Boeglin WE, Brash AR, Beier DR. A mouse mutation in the 12R-lipoxygenase, Alox12b, disrupts formation of the epidermal permeability barrier. J Invest Dermatol. 2007 Aug; 127(8):1893-7.
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  39. Ackerman KG, Wang J, Luo L, Fujiwara Y, Orkin SH, Beier DR. Gata4 is necessary for normal pulmonary lobar development. Am J Respir Cell Mol Biol. 2007 Apr; 36(4):391-7.
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  40. Ideraabdullah FY, Kim K, Pomp D, Moran JL, Beier D, de Villena FP. Rescue of the mouse DDK syndrome by parent-of-origin-dependent modifiers. Biol Reprod. 2007 Feb; 76(2):286-93.
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  41. Holland KD, Fleming MT, Cheek S, Moran JL, Beier DR, Meisler MH. De novo exon duplication in a new allele of mouse Glra1 (spasmodic). Genetics. 2006 Dec; 174(4):2245-7.
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  42. Lehoczky JA, Cai WW, Douglas JA, Moran JL, Beier DR, Innis JW. Description and genetic mapping of Polypodia: an X-linked dominant mouse mutant with ectopic caudal limbs and other malformations. Mamm Genome. 2006 Sep; 17(9):903-13.
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  43. Smith LA, Bukanov NO, Husson H, Russo RJ, Barry TC, Taylor AL, Beier DR, Ibraghimov-Beskrovnaya O. Development of polycystic kidney disease in juvenile cystic kidney mice: insights into pathogenesis, ciliary abnormalities, and common features with human disease. J Am Soc Nephrol. 2006 Oct; 17(10):2821-31.
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  44. Moran JL, Bolton AD, Tran PV, Brown A, Dwyer ND, Manning DK, Bjork BC, Li C, Montgomery K, Siepka SM, Vitaterna MH, Takahashi JS, Wiltshire T, Kwiatkowski DJ, Kucherlapati R, Beier DR. Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse. Genome Res. 2006 Mar; 16(3):436-40.
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  45. Fatma N, Kubo E, Sharma P, Beier DR, Singh DP. Impaired homeostasis and phenotypic abnormalities in Prdx6-/-mice lens epithelial cells by reactive oxygen species: increased expression and activation of TGFbeta. Cell Death Differ. 2005 Jul; 12(7):734-50.
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  46. Ackerman KG, Herron BJ, Vargas SO, Huang H, Tevosian SG, Kochilas L, Rao C, Pober BR, Babiuk RP, Epstein JA, Greer JJ, Beier DR. Fog2 is required for normal diaphragm and lung development in mice and humans. PLoS Genet. 2005 Jul; 1(1):58-65.
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  47. Herron BJ, Rao C, Liu S, Laprade L, Richardson JA, Olivieri E, Semsarian C, Millar SE, Stubbs L, Beier DR. A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice. Hum Mol Genet. 2005 Mar 1; 14(5):667-77.
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  48. Ackerman KG, Huang H, Grasemann H, Puma C, Singer JB, Hill AE, Lander E, Nadeau JH, Churchill GA, Drazen JM, Beier DR. Interacting genetic loci cause airway hyperresponsiveness. Physiol Genomics. 2005 Mar 21; 21(1):105-11.
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  49. Monti G, Schrijver R, Beier D. Genetic diversity and spread of Bovine leukaemia virus isolates in Argentine dairy cattle. Arch Virol. 2005 Mar; 150(3):443-58.
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  50. Beier DR, Herron BJ. Genetic mapping and ENU mutagenesis. Genetica. 2004 Sep; 122(1):65-9.
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  51. McDonald JD, Beier D. ENU mutagenesis in the mouse. Curr Protoc Hum Genet. 2004 Feb; Chapter 15:Unit 15.4.
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  52. Limanskii AP, Geue L, Limanskaia OIu, Beier D. [Typing of cattle leukemia virus circulating in the Ukraine]. Vopr Virusol. 2004 Jan-Feb; 49(1):39-44.
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  53. Beier DR, Dluhy RG. Bench and bedside--the G protein-coupled receptor GPR54 and puberty. N Engl J Med. 2003 Oct 23; 349(17):1589-92.
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  54. Rao C, Foernzler D, Loftus SK, Liu S, McPherson JD, Jungers KA, Apte SS, Pavan WJ, Beier DR. A defect in a novel ADAMTS family member is the cause of the belted white-spotting mutation. Development. 2003 Oct; 130(19):4665-72.
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  55. Carroll EA, Gerrelli D, Gasca S, Berg E, Beier DR, Copp AJ, Klingensmith J. Cordon-bleu is a conserved gene involved in neural tube formation. Dev Biol. 2003 Oct 1; 262(1):16-31.
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  56. Layer K, Lin G, Nencioni A, Hu W, Schmucker A, Antov AN, Li X, Takamatsu S, Chevassut T, Dower NA, Stang SL, Beier D, Buhlmann J, Bronson RT, Elkon KB, Stone JC, Van Parijs L, Lim B. Autoimmunity as the consequence of a spontaneous mutation in Rasgrp1. Immunity. 2003 Aug; 19(2):243-55.
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  57. Li Z, Stuart RO, Eraly SA, Gittes G, Beier DR, Nigam SK. Debt91, a putative zinc finger protein differentially expressed during epithelial morphogenesis. Biochem Biophys Res Commun. 2003 Jul 4; 306(3):623-8.
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  58. Beier DR. ENU mutagenesis: a work in progress. Physiol Genomics. 2002 Dec 3; 11(3):111-3.
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  59. Liu S, Lu W, Obara T, Kuida S, Lehoczky J, Dewar K, Drummond IA, Beier DR. A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish. Development. 2002 Dec; 129(24):5839-46.
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  60. Schymeinsky J, Nedbal S, Miosge N, Pöschl E, Rao C, Beier DR, Skarnes WC, Timpl R, Bader BL. Gene structure and functional analysis of the mouse nidogen-2 gene: nidogen-2 is not essential for basement membrane formation in mice. Mol Cell Biol. 2002 Oct; 22(19):6820-30.
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  61. Sun Y, Zhou J, Stayner C, Munasinghe J, Shen X, Beier DR, Albert MS. Magnetic resonance imaging assessment of a murine model of recessive polycystic kidney disease. Comp Med. 2002 Oct; 52(5):433-8.
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  62. Phelan SA, Beier DR, Higgins DC, Paigen B. Confirmation and high resolution mapping of an atherosclerosis susceptibility gene in mice on Chromosome 1. Mamm Genome. 2002 Oct; 13(10):548-53.
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  63. Beyer J, Köllner B, Teifke JP, Starick E, Beier D, Reimann I, Grunwald U, Ziller M. Cattle infected with bovine leukaemia virus may not only develop persistent B-cell lymphocytosis but also persistent B-cell lymphopenia. J Vet Med B Infect Dis Vet Public Health. 2002 Aug; 49(6):270-7.
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  64. Sweet DH, Miller DS, Pritchard JB, Fujiwara Y, Beier DR, Nigam SK. Impaired organic anion transport in kidney and choroid plexus of organic anion transporter 3 (Oat3 (Slc22a8)) knockout mice. J Biol Chem. 2002 Jul 26; 277(30):26934-43.
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  65. Zaghawa A, Beier D, Abd El-Rahim IH, Karim I, El-ballal S, Conraths FJ, Marquardt O. An outbreak of enzootic bovine leukosis in upper Egypt: clinical, laboratory and molecular-epidemiological studies. J Vet Med B Infect Dis Vet Public Health. 2002 Apr; 49(3):123-9.
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  66. Mátés L, Korpos E, Déak F, Liu Z, Beier DR, Aszódi A, Kiss I. Comparative analysis of the mouse and human genes (Matn2 and MATN2) for matrilin-2, a filament-forming protein widely distributed in extracellular matrices. Matrix Biol. 2002 Mar; 21(2):163-74.
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  67. Hou X, Mrug M, Yoder BK, Lefkowitz EJ, Kremmidiotis G, D'Eustachio P, Beier DR, Guay-Woodford LM. Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease. J Clin Invest. 2002 Feb; 109(4):533-40.
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  68. Lee ML, Lu W, Whitmore GA, Beier D. Models for microarray gene expression data. J Biopharm Stat. 2002 Feb; 12(1):1-19.
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  69. Beier DR, Herron BJ. 2001: a mouse genome odyssey. Genome Biol. 2002; 3(2):REPORTS4005.
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  70. Herron BJ, Lu W, Rao C, Liu S, Peters H, Bronson RT, Justice MJ, McDonald JD, Beier DR. Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis. Nat Genet. 2002 Feb; 30(2):185-9.
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  71. Fröhlich L, Liu Z, Beier DR, Lanske B. Genomic structure and refined chromosomal localization of the mouse Ptch2 gene. Cytogenet Genome Res. 2002; 97(1-2):106-10.
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  72. Stuart RO, Pavlova A, Beier D, Li Z, Krijanovski Y, Nigam SK. EEG1, a putative transporter expressed during epithelial organogenesis: comparison with embryonic transporter expression during nephrogenesis. Am J Physiol Renal Physiol. 2001 Dec; 281(6):F1148-56.
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  73. Chen F, Collin GB, Liu KC, Beier DR, Eccles M, Nishina PM, Moshang T, Epstein JA. Characterization of the murine Lbx2 promoter, identification of the human homologue, and evaluation as a candidate for Alström syndrome. Genomics. 2001 Jun 1; 74(2):219-27.
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  74. Nadeau JH, Balling R, Barsh G, Beier D, Brown SD, Bucan M, Camper S, Carlson G, Copeland N, Eppig J, Fletcher C, Frankel WN, Ganten D, Goldowitz D, Goodnow C, Guenet JL, Hicks G, Hrabe de Angelis M, Jackson I, Jacob HJ, Jenkins N, Johnson D, Justice M, Kay S, Kingsley D, Lehrach H, Magnuson T, Meisler M, Poustka A, Rinchik EM, Rossant J, Russell LB, Schimenti J, Shiroishi T, Skarnes WC, Soriano P, Stanford W, Takahashi JS, Wurst W, Zimmer A. Sequence interpretation. Functional annotation of mouse genome sequences. Science. 2001 Feb 16; 291(5507):1251-5.
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  75. Cho Y, Ramer J, Rivailler P, Quink C, Garber RL, Beier DR, Wang F. An Epstein-Barr-related herpesvirus from marmoset lymphomas. Proc Natl Acad Sci U S A. 2001 Jan 30; 98(3):1224-9.
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  76. Mrug M, Green WJ, DasGupta S, Beier DR, Lu W, D'Eustachio P, Guay-Woodford LM. An integrated genetic and physical map of the 650-kb region containing the congenital polycystic kidney (cpk) locus on mouse chromosome 12. Cytogenet Cell Genet. 2001; 94(1-2):55-61.
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  77. Jilek A, Engel E, Beier D, Lepperdinger G. Murine Bv8 gene maps near a synteny breakpoint of mouse chromosome 6 and human 3p21. Gene. 2000 Oct 3; 256(1-2):189-95.
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  78. Beier DR. Sequence-based analysis of mutagenized mice. Mamm Genome. 2000 Jul; 11(7):594-7.
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  79. Blankenstein P, Bondzio A, Fechner H, Beier D, Marquardt O, Looman AC, Ebner D. A nucleotide deletion causing a translational stop in the protease reading frame of bovine leukaemia virus (BLV) results in modified protein expression and loss of infectivity. J Vet Med B Infect Dis Vet Public Health. 2000 Jun; 47(5):361-71.
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  80. Beier D, Frank R. Molecular characterization of two-component systems of Helicobacter pylori. J Bacteriol. 2000 Apr; 182(8):2068-76.
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  81. Pavlova A, Sakurai H, Leclercq B, Beier DR, Yu AS, Nigam SK. Developmentally regulated expression of organic ion transporters NKT (OAT1), OCT1, NLT (OAT2), and Roct. Am J Physiol Renal Physiol. 2000 Apr; 278(4):F635-43.
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  82. Guay-Woodford LM, Green WJ, Lindsey JR, Beier DR. Germline and somatic loss of function of the mouse cpk gene causes biliary ductal pathology that is genetically modulated. Hum Mol Genet. 2000 Mar 22; 9(5):769-78.
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  83. Wagener R, Kobbe B, Aszódi A, Liu Z, Beier DR, Paulsson M. Structure and mapping of the mouse matrilin-3 gene (Matn3), a member of a gene family containing a U12-type AT-AC intron. Mamm Genome. 2000 Feb; 11(2):85-90.
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  84. Kuida S, Beier DR. Genetic localization of interacting modifiers affecting severity in a murine model of polycystic kidney disease. Genome Res. 2000 Jan; 10(1):49-54.
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  85. De Sanctis GT, Singer JB, Jiao A, Yandava CN, Lee YH, Haynes TC, Lander ES, Beier DR, Drazen JM. Quantitative trait locus mapping of airway responsiveness to chromosomes 6 and 7 in inbred mice. Am J Physiol. 1999 Dec; 277(6 Pt 1):L1118-23.
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  86. Cohen DE, Green RM, Wu MK, Beier DR. Cloning, tissue-specific expression, gene structure and chromosomal localization of human phosphatidylcholine transfer protein. Biochim Biophys Acta. 1999 Oct 28; 1447(2-3):265-70.
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  87. Iakoubova O, Dushkin H, Pacella L, Beier DR. Genetic analysis of modifying loci on mouse chromosome 1 that affect disease severity in a model of recessive PKD. Physiol Genomics. 1999 Aug 31; 1(2):101-5.
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  88. Dangond F, Foerznler D, Weremowicz S, Morton CC, Beier DR, Gullans SR. Cloning and expression of a murine histone deacetylase 3 (mHdac3) cDNA and mapping to a region of conserved synteny between murine chromosome 18 and human chromosome 5. Mol Cell Biol Res Commun. 1999 Aug; 2(2):91-6.
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  89. Marks PW, Bandura JL, Shieh DB, Foernzler D, Beier DR, Kwiatkowski DJ. The spontaneous coat color mutant white nose (wn) maps to murine chromosome 15. Mamm Genome. 1999 Jul; 10(7):750-2.
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  90. Schön MP, Arya A, Murphy EA, Adams CM, Strauch UG, Agace WW, Marsal J, Donohue JP, Her H, Beier DR, Olson S, Lefrancois L, Brenner MB, Grusby MJ, Parker CM. Mucosal T lymphocyte numbers are selectively reduced in integrin alpha E (CD103)-deficient mice. J Immunol. 1999 Jun 1; 162(11):6641-9.
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  91. Kvist AP, Latvanlehto A, Sund M, Horelli-Kuitunen N, Rehn M, Palotie A, Beier D, Pihlajaniemi T. Complete exon-intron organization and chromosomal location of the gene for mouse type XIII collagen (col13a1) and comparison with its human homologue. Matrix Biol. 1999 Jun; 18(3):261-74.
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  92. Green RM, Lo K, Sterritt C, Beier DR. Cloning and functional expression of a mouse liver organic cation transporter. Hepatology. 1999 May; 29(5):1556-62.
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  93. In KH, Silverman ES, Asano K, Beier D, Fischer AR, Keith TP, Serino K, Yandava C, De Sanctis GT, Drazen JM. Mutations in the human 5-lipoxygenase gene. Clin Rev Allergy Immunol. 1999 Spring-Summer; 17(1-2):59-69.
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  94. Brady KP, Dushkin H, Förnzler D, Koike T, Magner F, Her H, Gullans S, Segre GV, Green RM, Beier DR. A novel putative transporter maps to the osteosclerosis (oc) mutation and is not expressed in the oc mutant mouse. Genomics. 1999 Mar 15; 56(3):254-61.
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  95. Mount DB, Baekgaard A, Hall AE, Plata C, Xu J, Beier DR, Gamba G, Hebert SC. Isoforms of the Na-K-2Cl cotransporter in murine TAL I. Molecular characterization and intrarenal localization. Am J Physiol. 1999 Mar; 276(3 Pt 2):F347-58.
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  96. Davidson AJ, Postlethwait JH, Yan YL, Beier DR, van Doren C, Foernzler D, Celeste AJ, Crosier KE, Crosier PS. Isolation of zebrafish gdf7 and comparative genetic mapping of genes belonging to the growth/differentiation factor 5, 6, 7 subgroup of the TGF-beta superfamily. Genome Res. 1999 Feb; 9(2):121-9.
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  97. Deák F, Mátés L, Krysan K, Liu Z, Szabó PE, Mann JR, Beier DR, Kiss I. Characterization and chromosome location of the mouse link protein gene (Crtl1). Cytogenet Cell Genet. 1999; 87(1-2):75-9.
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  98. Foernzler D, Beier DR. Gene mapping in zebrafish using single-strand conformation polymorphism analysis. Methods Cell Biol. 1999; 60:185-93.
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  99. Phelan SA, Johnson KA, Beier DR, Paigen B. Characterization of the murine gene encoding Aop2 (antioxidant protein 2) and identification of two highly related genes. Genomics. 1998 Nov 15; 54(1):132-9.
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  100. Twist CJ, Beier DR, Disteche CM, Edelhoff S, Tedder TF. The mouse Cd83 gene: structure, domain organization, and chromosome localization. Immunogenetics. 1998 Nov-Dec; 48(6):383-93.
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  101. Strobl B, Wechselberger C, Beier DR, Lepperdinger G. Structural organization and chromosomal localization of Hyal2, a gene encoding a lysosomal hyaluronidase. Genomics. 1998 Oct 15; 53(2):214-9.
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  102. Beier D, Spohn G, Rappuoli R, Scarlato V. Functional analysis of the Helicobacter pylori principal sigma subunit of RNA polymerase reveals that the spacer region is important for efficient transcription. Mol Microbiol. 1998 Oct; 30(1):121-34.
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  103. Donaldson DD, Whitters MJ, Fitz LJ, Neben TY, Finnerty H, Henderson SL, O'Hara RM, Beier DR, Turner KJ, Wood CR, Collins M. The murine IL-13 receptor alpha 2: molecular cloning, characterization, and comparison with murine IL-13 receptor alpha 1. J Immunol. 1998 Sep 1; 161(5):2317-24.
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  104. Heaney C, Shalev H, Elbedour K, Carmi R, Staack JB, Sheffield VC, Beier DR. Human autosomal recessive osteopetrosis maps to 11q13, a position predicted by comparative mapping of the murine osteosclerosis (oc) mutation. Hum Mol Genet. 1998 Sep; 7(9):1407-10.
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  105. Förnzler D, Her H, Knapik EW, Clark M, Lehrach H, Postlethwait JH, Zon LI, Beier DR. Gene mapping in zebrafish using single-strand conformation polymorphism analysis. Genomics. 1998 Jul 15; 51(2):216-22.
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  106. Green RM, Ananthanarayanan M, Suchy FJ, Beier DR. Genetic mapping of the Na(+)-taurocholate cotransporting polypeptide to mouse chromosome 12. Mamm Genome. 1998 Jul; 9(7):598.
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  107. Thompson MA, Ransom DG, Pratt SJ, MacLennan H, Kieran MW, Detrich HW, Vail B, Huber TL, Paw B, Brownlie AJ, Oates AC, Fritz A, Gates MA, Amores A, Bahary N, Talbot WS, Her H, Beier DR, Postlethwait JH, Zon LI. The cloche and spadetail genes differentially affect hematopoiesis and vasculogenesis. Dev Biol. 1998 May 15; 197(2):248-69.
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  108. Blankenstein P, Fechner H, Looman AC, Beier D, Marquardt O, Ebner D. [Polymerase chain reaction (PCR) for detection of BLV provirus-- a practical complement for BLV diagnosis?]. Berl Munch Tierarztl Wochenschr. 1998 May; 111(5):180-6.
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  109. Postlethwait JH, Yan YL, Gates MA, Horne S, Amores A, Brownlie A, Donovan A, Egan ES, Force A, Gong Z, Goutel C, Fritz A, Kelsh R, Knapik E, Liao E, Paw B, Ransom D, Singer A, Thomson M, Abduljabbar TS, Yelick P, Beier D, Joly JS, Larhammar D, Rosa F, Westerfield M, Zon LI, Johnson SL, Talbot WS. Vertebrate genome evolution and the zebrafish gene map. Nat Genet. 1998 Apr; 18(4):345-9.
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  110. Aszódi A, Beier DR, Hiripi L, Bösze Z, Fässler R. Sequence, structure and chromosomal localization of Crtm gene encoding mouse cartilage matrix protein and its exclusion as a candidate for murine achondroplasia. Matrix Biol. 1998 Mar; 16(9):563-73.
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  111. Neuhaus IM, Beier DR. Efficient localization of mutations by interval haplotype analysis. Mamm Genome. 1998 Feb; 9(2):150-4.
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  112. Lammert F, Cohen DE, Paigen B, Carey MC, Beier DR. The gene encoding the multispecific organic anion transporter (Cmoat) of the hepatocyte canalicular membrane maps to mouse chromosome 19. Mamm Genome. 1998 Jan; 9(1):87-8.
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  113. Beier DR. Zebrafish: genomics on the fast track. Genome Res. 1998 Jan; 8(1):9-17.
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  114. Landgren C, Beier DR, Fässler R, Heinegård D, Sommarin Y. The mouse chondroadherin gene: characterization and chromosomal localization. Genomics. 1998 Jan 1; 47(1):84-91.
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  115. Drazen JM, Beier DR. The genetics of air pollution. Nat Genet. 1997 Dec; 17(4):365-6.
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  116. Skvorak AB, Robertson NG, Yin Y, Weremowicz S, Her H, Bieber FR, Beisel KW, Lynch ED, Beier DR, Morton CC. An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1). Genomics. 1997 Dec 1; 46(2):191-9.
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  117. Brady KP, Rowe LB, Her H, Stevens TJ, Eppig J, Sussman DJ, Sikela J, Beier DR. Genetic mapping of 262 loci derived from expressed sequences in a murine interspecific cross using single-strand conformational polymorphism analysis. Genome Res. 1997 Nov; 7(11):1085-93.
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  118. Fechner H, Blankenstein P, Looman AC, Elwert J, Geue L, Albrecht C, Kurg A, Beier D, Marquardt O, Ebner D. Provirus variants of the bovine leukemia virus and their relation to the serological status of naturally infected cattle. Virology. 1997 Oct 27; 237(2):261-9.
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  119. Bui TD, Beier DR, Jonssen M, Smith K, Dorrington SM, Kaklamanis L, Kearney L, Regan R, Sussman DJ, Harris AL. cDNA cloning of a human dishevelled DVL-3 gene, mapping to 3q27, and expression in human breast and colon carcinomas. Biochem Biophys Res Commun. 1997 Oct 20; 239(2):510-6.
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  120. Apte SS, Fukai N, Beier DR, Olsen BR. The matrix metalloproteinase-14 (MMP-14) gene is structurally distinct from other MMP genes and is co-expressed with the TIMP-2 gene during mouse embryogenesis. J Biol Chem. 1997 Oct 10; 272(41):25511-7.
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  121. Iakoubova OA, Dushkin H, Beier DR. Genetic analysis of a quantitative trait in a mouse model of polycystic kidney disease. Am J Respir Crit Care Med. 1997 Oct; 156(4 Pt 2):S72-7.
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  122. Green RM, Gollan JL, Hagenbuch B, Meier PJ, Beier DR. Regulation of hepatocyte bile salt transporters during hepatic regeneration. Am J Physiol. 1997 Sep; 273(3 Pt 1):G621-7.
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  123. Rauch U, Meyer H, Brakebusch C, Seidenbecher C, Gundelfinger ED, Beier DR, Fässler R. Sequence and chromosomal localization of the mouse brevican gene. Genomics. 1997 Aug 15; 44(1):15-21.
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  124. Fleming MD, Trenor CC, Su MA, Foernzler D, Beier DR, Dietrich WF, Andrews NC. Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene. Nat Genet. 1997 Aug; 16(4):383-6.
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  125. Beier D, Spohn G, Rappuoli R, Scarlato V. Identification and characterization of an operon of Helicobacter pylori that is involved in motility and stress adaptation. J Bacteriol. 1997 Aug; 179(15):4676-83.
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  126. Fitz LJ, Morris JC, Towler P, Long A, Burgess P, Greco R, Wang J, Gassaway R, Nickbarg E, Kovacic S, Ciarletta A, Giannotti J, Finnerty H, Zollner R, Beier DR, Leak LV, Turner KJ, Wood CR. Characterization of murine Flt4 ligand/VEGF-C. Oncogene. 1997 Jul 31; 15(5):613-8.
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  127. Neuhaus IM, Sommardahl CS, Johnson DK, Beier DR. Microsatellite DNA variants between the FVB/N and C3HeB/FeJLe and C57BL/6J mouse strains. Mamm Genome. 1997 Jul; 8(7):506-9.
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  128. Iakoubova OA, Pacella LA, Her H, Beier DR. LTW4 protein on mouse chromosome 1 is a member of a family of antioxidant proteins. Genomics. 1997 Jun 15; 42(3):474-8.
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  129. Lopez-Nieto CE, You G, Bush KT, Barros EJ, Beier DR, Nigam SK. Molecular cloning and characterization of NKT, a gene product related to the organic cation transporter family that is almost exclusively expressed in the kidney. J Biol Chem. 1997 Mar 7; 272(10):6471-8.
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  130. In KH, Asano K, Beier D, Grobholz J, Finn PW, Silverman EK, Silverman ES, Collins T, Fischer AR, Keith TP, Serino K, Kim SW, De Sanctis GT, Yandava C, Pillari A, Rubin P, Kemp J, Israel E, Busse W, Ledford D, Murray JJ, Segal A, Tinkleman D, Drazen JM. Naturally occurring mutations in the human 5-lipoxygenase gene promoter that modify transcription factor binding and reporter gene transcription. J Clin Invest. 1997 Mar 1; 99(5):1130-7.
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  131. Xu PX, Woo I, Her H, Beier DR, Maas RL. Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode. Development. 1997 Jan; 124(1):219-31.
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  132. Fechner H, Kurg A, Geue L, Blankenstein P, Mewes G, Ebner D, Beier D. Evaluation of polymerase chain reaction (PCR) application in diagnosis of bovine leukaemia virus (BLV) infection in naturally infected cattle. Zentralbl Veterinarmed B. 1996 Dec; 43(10):621-30.
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  133. Tsang M, Lijam N, Yang Y, Beier DR, Wynshaw-Boris A, Sussman DJ. Isolation and characterization of mouse dishevelled-3. Dev Dyn. 1996 Nov; 207(3):253-62.
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  134. Morris JC, Neben S, Bennett F, Finnerty H, Long A, Beier DR, Kovacic S, McCoy JM, DiBlasio-Smith E, La Vallie ER, Caruso A, Calvetti J, Morris G, Weich N, Paul SR, Crosier PS, Turner KJ, Wood CR. Molecular cloning and characterization of murine interleukin-11. Exp Hematol. 1996 Oct; 24(12):1369-76.
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  135. Beier D, Deppisch H, Gross R. Conserved sequence motifs in the unorthodox BvgS two-component sensor protein of Bordetella pertussis. Mol Gen Genet. 1996 Aug 27; 252(1-2):169-76.
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  136. Klingensmith J, Yang Y, Axelrod JD, Beier DR, Perrimon N, Sussman DJ. Conservation of dishevelled structure and function between flies and mice: isolation and characterization of Dvl2. Mech Dev. 1996 Aug; 58(1-2):15-26.
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  137. Beier DR, Dushkin H, Stone LV, Sherman GF. A transgene insertion at perinatal lethality (ple) is associated with abnormalities of the cortex. Brain Res. 1996 Jul 15; 727(1-2):196-204.
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  138. Green RM, Beier D, Gollan JL. Regulation of hepatocyte bile salt transporters by endotoxin and inflammatory cytokines in rodents. Gastroenterology. 1996 Jul; 111(1):193-8.
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  139. Beier D, Fuchs TM, Graeff-Wohlleben H, Gross R. Signal transduction and virulence regulation in Bordetella pertussis. Microbiologia. 1996 Jun; 12(2):185-96.
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  140. De Sanctis GT, Merchant M, Beier DR, Dredge RD, Grobholz JK, Martin TR, Lander ES, Drazen JM. Quantitative locus analysis of airway hyperresponsiveness in A/J and C57BL/6J mice. Nat Genet. 1995 Oct; 11(2):150-4.
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  141. Rauch U, Grimpe B, Kulbe G, Arnold-Ammer I, Beier DR, Fässler R. Structure and chromosomal localization of the mouse neurocan gene. Genomics. 1995 Aug 10; 28(3):405-10.
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  142. Chen H, Thalmann I, Adams JC, Avraham KB, Copeland NG, Jenkins NA, Beier DR, Corey DP, Thalmann R, Duyk GM. cDNA cloning, tissue distribution, and chromosomal localization of Ocp2, a gene encoding a putative transcription-associated factor predominantly expressed in the auditory organs. Genomics. 1995 Jun 10; 27(3):389-98.
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  143. Beier D, Schwarz B, Fuchs TM, Gross R. In vivo characterization of the unorthodox BvgS two-component sensor protein of Bordetella pertussis. J Mol Biol. 1995 May 5; 248(3):596-610.
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  144. Beier DR, Dushkin H, Telle T. Haplotype analysis of intra-specific backcross curly-tail mice confirms the localization of ct to chromosome 4. Mamm Genome. 1995 Apr; 6(4):269-72.
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  145. Iakoubova OA, Dushkin H, Beier DR. Localization of a murine recessive polycystic kidney disease mutation and modifying loci that affect disease severity. Genomics. 1995 Mar 1; 26(1):107-14.
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  146. Li Y, Lacerda DA, Warman ML, Beier DR, Yoshioka H, Ninomiya Y, Oxford JT, Morris NP, Andrikopoulos K, Ramirez F, et al. A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis. Cell. 1995 Feb 10; 80(3):423-30.
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  147. Green RM, Whiting JF, Rosenbluth AB, Beier D, Gollan JL. Interleukin-6 inhibits hepatocyte taurocholate uptake and sodium-potassium-adenosinetriphosphatase activity. Am J Physiol. 1994 Dec; 267(6 Pt 1):G1094-100.
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  148. Delpire E, Rauchman MI, Beier DR, Hebert SC, Gullans SR. Molecular cloning and chromosome localization of a putative basolateral Na(+)-K(+)-2Cl- cotransporter from mouse inner medullary collecting duct (mIMCD-3) cells. J Biol Chem. 1994 Oct 14; 269(41):25677-83.
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  149. Warman ML, McCarthy MT, Perälä M, Vuorio E, Knoll JH, McDaniels CN, Mayne R, Beier DR, Olsen BR. The genes encoding alpha 2(IX) collagen (COL9A2) map to human chromosome 1p32.3-p33 and mouse chromosome 4. Genomics. 1994 Sep 1; 23(1):158-62.
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  150. Kaiser UB, Dushkin H, Altherr MR, Beier DR, Chin WW. Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13.1-q21.1 and mouse chromosome 5. Genomics. 1994 Apr; 20(3):506-8.
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  151. Sherman GF, Stone LV, Denenerg VH, Beier DR. A genetic analysis of neocortical ectopias in New Zealand black autoimmune mice. Neuroreport. 1994 Feb 24; 5(6):721-4.
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  152. Crosier PS, Lewis PM, Hall LR, Vitas MR, Morris CM, Beier DR, Wood CR, Crosier KE. Isolation of a receptor tyrosine kinase (DTK) from embryonic stem cells: structure, genetic mapping and analysis of expression. Growth Factors. 1994; 11(2):125-36.
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  153. Ord DC, Edelhoff S, Dushkin H, Zhou LJ, Beier DR, Disteche C, Tedder TF. CD19 maps to a region of conservation between human chromosome 16 and mouse chromosome 7. Immunogenetics. 1994; 39(5):322-8.
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  154. Peichel CL, Scherer SW, Tsui LC, Beier DR, Vogt TF. Mapping the midkine family of developmentally regulated signaling molecules. Mamm Genome. 1993 Nov; 4(11):632-8.
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  155. Beier DR. Single-strand conformation polymorphism (SSCP) analysis as a tool for genetic mapping. Mamm Genome. 1993 Nov; 4(11):627-31.
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  156. Shultz LD, Schweitzer PA, Rajan TV, Yi T, Ihle JN, Matthews RJ, Thomas ML, Beier DR. Mutations at the murine motheaten locus are within the hematopoietic cell protein-tyrosine phosphatase (Hcph) gene. Cell. 1993 Jul 2; 73(7):1445-54.
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  157. Atala A, Freeman MR, Mandell J, Beier DR. Juvenile cystic kidneys (jck): a new mouse mutation which causes polycystic kidneys. Kidney Int. 1993 May; 43(5):1081-5.
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  158. Fuchs T, Beier D, Beier H. The tRNA(Tyr) multigene family of Nicotiana rustica: genome organization, sequence analyses and expression in vitro. Plant Mol Biol. 1992 Dec; 20(5):869-78.
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  159. Stange N, Beier D, Beier H. Intron excision from tRNA precursors by plant splicing endonuclease requires unique features of the mature tRNA domain. Eur J Biochem. 1992 Nov 15; 210(1):193-203.
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  160. Beier DR, Dushkin H, Sussman DJ. Mapping genes in the mouse using single-strand conformation polymorphism analysis of recombinant inbred strains and interspecific crosses. Proc Natl Acad Sci U S A. 1992 Oct 1; 89(19):9102-6.
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  161. Beier D, Beier H. Expression of variant nuclear Arabidopsis tRNA(Ser) genes and pre-tRNA maturation differ in HeLa, yeast and wheat germ extracts. Mol Gen Genet. 1992 May; 233(1-2):201-8.
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  162. Beier DR, Chaillet JR, Schmidt EV, Leder P. Close linkage of a transgene insertion site to the steel (Sl) locus on mouse chromosome 10. Genomics. 1991 Aug; 10(4):1003-8.
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  163. Chaillet JR, Vogt TF, Beier DR, Leder P. Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis. Cell. 1991 Jul 12; 66(1):77-83.
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  164. Stange N, Beier D, Beier H. Expression of nuclear tRNA(Tyr) genes from Arabidopsis thaliana in HeLa cell and wheat germ extracts. Plant Mol Biol. 1991 May; 16(5):865-75.
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  165. Beier D, Stange N, Gross HJ, Beier H. Nuclear tRNA(Tyr) genes are highly amplified at a single chromosomal site in the genome of Arabidopsis thaliana. Mol Gen Genet. 1991 Jan; 225(1):72-80.
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  166. Huang E, Nocka K, Beier DR, Chu TY, Buck J, Lahm HW, Wellner D, Leder P, Besmer P. The hematopoietic growth factor KL is encoded by the Sl locus and is the ligand of the c-kit receptor, the gene product of the W locus. Cell. 1990 Oct 5; 63(1):225-33.
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  167. Beier DR, Morton CC, Leder A, Wallace R, Leder P. Perinatal lethality (ple): a mutation caused by integration of a transgene into distal mouse chromosome 15. Genomics. 1989 May; 4(4):498-504.
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  168. Williams DA, Rosenblatt MF, Beier DR, Cone RD. Generation of murine stromal cell lines supporting hematopoietic stem cell proliferation by use of recombinant retrovirus vectors encoding simian virus 40 large T antigen. Mol Cell Biol. 1988 Sep; 8(9):3864-71.
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  169. Beier DR, Sledziewski A, Young ET. Deletion analysis identifies a region, upstream of the ADH2 gene of Saccharomyces cerevisiae, which is required for ADR1-mediated derepression. Mol Cell Biol. 1985 Jul; 5(7):1743-9.
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